A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162181



Internal ID20729221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108223701..108224800hg38UCSC Ensembl
chr8:109235930..109237029hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421029
Supporting Variants
Samples
Known GenesEIF3E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0097


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